@article{6b1649395afd40c5a63715f67d894d44,
title = "Circulating miR-216a as a biomarker of metabolic alterations and obesity in women",
abstract = "Obesity leads to an amplified risk of disease and contributes to the occurrence of type 2 diabetes, fatty liver disease, coronary heart disease, stroke, chronic kidney disease and various types of cancer. MicroRNAs (miRNAs), small non-coding RNA molecules of 20-25 nucleotides, can remain stable in plasma and have been studied as potential (predictive) biomarkers for obesity and related metabolic disorders. The aim of this study was to identify circulating miRNAs as biomarkers for obesity status and metabolic alterations in women. Circulating miR-216a and miR-155-5p were selected by miRNA expression profiling and validated by real time quantitative PCR in a validation cohort of 60 obese women and 60 normal weight-age-matched control women. This was supplemented by correlation analysis of the candidate miRNA and anthropometric variables, blood biochemistry and lipid profile markers. Circulating miR-216a was validated as a biomarker of obesity status with significantly reduced levels in obese women. Interestingly, this was associated with a negative correlation between the plasma miR-216a content and body mass index (BMI), waist circumference, mean arterial pressure (MAP), triglycerides, ratio of total cholesterol/high density lipoprotein (HDL)-cholesterol and high sensitivity-C reactive protein (hs-CRP).Taken together, we provide evidence for an abnormally expressed circulating miRNA, miR-216a, with additive value as a predictive marker for obesity that correlates with metabolic alterations presented by lipid profile and inflammatory markers.",
keywords = "Biomarker, CLUSTERS, COMPARATIVE RISK-ASSESSMENT, DISEASE, GENE-EXPRESSION, GLOBAL BURDEN, MICRORNAS, MIRNAS, Metabolic syndrome, Obesity, PROFILE, SERUM, SYSTEMATIC ANALYSIS, microRNA, RISK, SAMPLE",
author = "Vonhogen, {Indira G. C.} and Zenab Mohseni and Bjorn Winkens and Ke Xiao and Thomas Thum and Martina Calore and Martins, {Paula A. da Costa} and {de Windt}, {Leon J.} and Spaanderman, {Marc E. A.} and Chahinda Ghossein-Doha",
note = "Funding Information: T.T. acknowledges support from the German Research Foundation ( KFO311 ). PDCM was supported by a MEERVOUD grant from the Dutch Research Council ( 2011/09039/ALW ) and is an Established Investigator of the Dutch Heart Foundation ( 2015T066 ). L.D.W. acknowledges support from the Netherlands CardioVascular Research Initiative: the Dutch Heart Foundation, Dutch Federation of University Medical Centers, ZonMW and the Royal Netherlands Academy of Sciences (ARENA-PRIME) . L.D.W. was supported by grant 311549 from the European Research Council (ERC) , a VICI award 918-156-47 from the Dutch Research Council (NWO) and the European Union{\textquoteright}s Horizon 2020 research and innovation programme under the Marie Sk{\l}odowska-Curie grant agreement No 813716 . Funding Information: T.T. acknowledges support from the German Research Foundation (KFO311). PDCM was supported by a MEERVOUD grant from the Dutch Research Council (2011/09039/ALW) and is an Established Investigator of the Dutch Heart Foundation (2015T066). L.D.W. acknowledges support from the Netherlands CardioVascular Research Initiative: the Dutch Heart Foundation, Dutch Federation of University Medical Centers, ZonMW and the Royal Netherlands Academy of Sciences (ARENA-PRIME). L.D.W. was supported by grant 311549 from the European Research Council (ERC), a VICI award 918-156-47 from the Dutch Research Council (NWO) and the European Union's Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No 813716. Publisher Copyright: {\textcopyright} 2020 [The Author/The Authors]",
year = "2020",
month = sep,
doi = "10.1016/j.ncrna.2020.08.001",
language = "English",
volume = "5",
pages = "144--152",
journal = "Non-Coding rna research",
issn = "2468-2160",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "3",
}